A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705129



Internal ID15441781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91084252..91096349hg38UCSC Ensembl
Innerchr4:92005403..92017500hg19UCSC Ensembl
Innerchr4:92224426..92236523hg18UCSC Ensembl
Innerchr4:92362581..92374678hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3812098
hg1912098
hg1812098
hg1712098
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528519
Supporting Variants
Samples
Known GenesCCSER1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705129
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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